From 2012.igem.org

Vector Design

Responsible: Ingmar Polte

What is the use of DNA sequences coding for valuable enzymes without the possibility to express them and analyze the protein activity?

As we planned to detect the enzymes from our biosynthetic pathways via Strep-tag II, a RFC25 compatible backbone was necessary. As no such backbone was availabe for yeast in the PartsRegistry, an important task at the beginning of our project was the design of an expression vector for yeast which is compatible to the iGEM cloning principles and standards. Based on the commercially available pYES2 vector, manufactured by Invitrogen, we created an vector containing:

• a RFC 25 compatible multiple cloning site
• a strep-tag II
• a 2µ origin for high copy number replication in Saccharomyces cerevisae
• the URA3 gene to use the uracil prototrophy of S. cerevisiae INVSc' as a selection marker for transfection
• a pUC origin for high copy number replication in E.coli
• the ß-lactamase coding gene to use ampicillin as a selection marker for cloning applications in E.coli
• a galacotsoe inducible PGal 1 promoter
• a CYC1 transcription terminator

Furthermore we designed several vectors containing our constitutive promoters Tef1, Tef2 and ADH and different additional terminators. The different versions of the vector have been successfully applied and tested in all other subprojects.

Design

Explanations on the figure: Figure A shows the commercial available pYES from Invitrogen on the left. The gel picture in the middle shows the successive deletion of forbidden restriction sides in the vector backbone. The colures of the annotations of the bonds in the gel picture are visualized in the graphic on the right by colored dived circles.

vom Poster:

RFC25 COMPATIBILITY

To be able to test and quantify the expression of desired enzymes in yeast we designed an expression vector which is compatible to the iGEM RFC25 standard based on the commercially available pYES2 vector from Invitrogen.

DESIGN

This included an exchange of the original multiple cloning site by a multiple cloning site consisting of the restriction enzymes used in the iGEM RFC25 standard. Additionally the restriction sites of these enzymes in the vector backbone have been eliminated by quick-change mutagenisis. Furthermore we inserted a gene sequence coding for a strep-tag II straight behind the multiple cloning site in order to facilitate the extraction of expressed proteins. The successful introduction of these modifications has been confirmed via DNA sequencing. Additionally a second vector containing a His-tag instead of the strep-tag II and a vector giving the opportunity to test different promoters is currently planned.

Description of the original vector + 4 different modified versions.

Results

BioBricks

Gel pictures of finished constructs

Characterization

Induction assays with galactose

Characterization of constitutive promoters

Reference